Tree peony (Paeonia sp.) is a popular traditional ornamental plant in China. Among the nine wild species, Paeonia rockii displays wide-ranging, deep purple variegation at the base of the petals, whereas Paeonia ostii exhibits purely white petals. Overall, the posttranscriptional regulation involved in tree peony flower opening and pigmentation remains unclear. To identify potential microRNAs (miRNAs) involved in flower variegation, six small RNA libraries of P. ostii and P. rockii petals at three different opening stages were constructed and sequenced. Using Illumina-based sequencing, 22 conserved miRNAs and 27 novel miRNAs were identified in P. rockii and P. ostii petals. Seventeen miRNAs were differentially expressed during flower development, and several putative target genes of these miRNAs belonged to transcription factor families, such as Myb domain (MYB), and basic helix-loop-helix (bHLH) transcription factors. Furthermore, an integrative analysis of the expression profiles of miRNAs and their corresponding target genes revealed that variegation formation might be regulated by miR159c, miR168, miR396a, and novel_miR_05, which target the MYB transcription factors, chalcone synthase (CHS), and ABC transporter. Our preliminary study is the first report of miRNAs involved in Paeonia flower pigmentation. It provides insight regarding the molecular mechanisms underlying the regulation of flower pigmentation in tree peony.
Qianqian Shi, Xiaoxiao Zhang, Xiang Li, Lijuan Zhai, Xiaoning Luo, Jianrang Luo, Lixia He, Yanlong Zhang and Long Li
Xiaoning Li, Xiaoyan Sun, Guangyang Wang, Erick Amombo, Xiuwen Zhou, Zhaohong Du, Yinkun Zhang, Yan Xie and Jinmin Fu
Phosphorus (P) is an essential nutrient element that is necessary for plant growth and development. However, most of the P exists in insoluble form. Aspergillus aculeatus has been reported to be able to solubilize insoluble forms of P. Here, to investigate the P-solubilizing effect of A. aculeatus on the performance of perennial ryegrass (Lolium perenne) under P-deficiency stress, we created four treatment groups: control [i.e., no Ca3(PO4)2 or A. aculeatus], A. aculeatus only (F), Ca3(PO4)2 and Ca3(PO4)2 + A. aculeatus [Ca3(PO4)2 + F] treatment, and Ca3(PO4)2 at concentrations of 0 and 3 g per pot (0.5 kg substrate per pot). In our results, the liquid medium inoculated with A. aculeatus exhibited enhanced soluble P and organic acid content (tartaric acid, citric acid, and aminoacetic acid) accompanied with lower pH, compared with the noninoculated regimen. Furthermore, A. aculeatus also played a primary role in increasing the soluble P content of substrate (1 sawdust: 3 sand), the growth rate, turf quality, and photosynthetic capacity of the plant exposed to Ca3(PO4)2 + F treatment, compared with other groups. Finally, in perennial ryegrass leaves, there was a dramatic increase in the valine, serine, tyrosine, and proline contents, and a remarkable decline in the glutamic acid, succinic acid, citric acid, and fumaric acid contents in the Ca3(PO4)2 + F regimen, compared with other groups. Overall, our results suggested that A. aculeatus may play a crucial role in the process of solubilizing Ca3(PO4)2 and modulating perennial ryegrass growth under P-deficiency stress.